This data was extracted from Medline abstracts and full texts (when available) in an automated manner.
The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation R83H was found are listed after the table.
The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.
|General numbering (KChannelDB):||-|
|Other point mutations / same protein / same position||Point mutations at position 83 in KCNE3_HUMAN|
|Other point mutations / same protein||List of mutations in KCNE3_HUMAN|
IsK related channels (minK,MiRP,AMMECR2)|
Potassium channels 1 TM
|Other point mutations / same position||
Position 69 in IsK related channels (minK,MiRP,AMMECR2) family |
Position 69 in Potassium channels 1 TM family
|Reference:||No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.|
Tang NL, Chow CC, Ko GT, Tai MH, Kwok R, Yao XQ, Cockram CS
Clin Endocrinol (Oxf) 2004 Jul;61(1):109-12.
|Other point mutations / same article||List|
|Text source||HTML full text|
|Validation status||Not yet checked|